A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598954



Internal ID6986002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184638587..184646181hg38UCSC Ensembl
Innerchr3:184638603..184646165hg38UCSC Ensembl
Outerchr3:184638571..184646197hg38UCSC Ensembl
chr3:184356375..184363969hg19UCSC Ensembl
Innerchr3:184356391..184363953hg19UCSC Ensembl
Outerchr3:184356359..184363985hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg387595
hg197595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11257572
SamplesNA19081
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598954
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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